My grandma Cita had the best laugh. It was infectious, warm, and full of love. It was a sound I will never forget and always miss. I grew up knowing exactly what ALS is and the progression of the disease. Many of grandma Cita's family members had the awful disease and had passed away from ALS or complications due to ALS.
Grandma Cita passed away this last June. Even though her death has been a mix of emotions for me, she is not suffering anymore and for that I can be greatful. However, there is still not a cure for ALS. With all the dontations from the Ice Bucket Challenge, they found a new gene that can be linked to ALS..... which means reachers are closer than ever to find a cure.
For this reason and so many others....
Please consider walking with me or sponsoring me. With your help, we will be able to make a difference in the lives of people affected by this disease.
Why We Need Your Help
Often referred to as Lou Gehrig's Disease, amyotrophic lateral sclerosis (ALS) is a progressive, fatal neuromuscular disease that slowly robs the body of its ability to walk, speak, swallow and breathe. The life expectancy of an ALS patient averages 2 to 5 years from the time of diagnosis.
Every 90 minutes a person in this country is diagnosed with ALS and every 90 minutes another person will lose their battle against this disease. ALS occurs throughout the world with no racial, ethnic, or socioeconomic boundaries.
This crippling disease can strike anyone. Presently there is no known cause of the disease though support is bringing researchers closer to an answer. In the mean time it costs an average of $200,000 a year to provide the care ALS patients need. Help make a difference and donate or join a walk today.
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